Behr Syndrome - Complicated hereditary infantile optic atrophy

Kleffner I., Meyer C., Gess B., Korsukewitz C., Allkemper T., Schirmacher A., Young P., Husstedt I. (2013)

In: Klinische Neurophysiologie, 44(1).

Research article (journal)

Enhanced rapid-onset cortical plasticity in CADASIL as a possible mechanism of preserved cognition.

List J, Duning T, Meinzer M, Kürten J, Schirmacher A, Deppe M, Evers S, Young P, Flöel A (2011)

In: Cerebral cortex, 21(12).

Research article (journal)

A novel splice site mutation in the SPG7 gene causing widespread fiber damage in homozygous and heterozygous subjects.

Warnecke T, Duning T, Schirmacher A, Mohammadi S, Schwindt W, Lohmann H, Dziewas R, Deppe M, Ringelstein EB, Young P (2010)

In: Movement Disorders, 25(4).

Research article (journal)

Four novel mutations of the myelin protein zero gene presenting as a mild and late-onset polyneuropathy.

Kleffner I, Schirmacher A, Gess B, Boentert M, Young P (2010)

In: Journal of Neurology, 257(11).

Research article (journal)

Mutations in SEPT9 cause hereditary neuralgic amyotrophy.

Kuhlenbäumer G, Hannibal MC, Nelis E, Schirmacher A, Verpoorten N, Meuleman J, Watts GD, De Vriendt E, Young P, Stögbauer F, Halfter H, Irobi J, Goossens D, Del-Favero J, Betz BG, Hor H, Kurlemann G, Bird TD, Airaksinen E, Mononen T, Serradell AP, Prats JM, Van Broeckhoven C, De Jonghe P, Timmerman V, Ringelstein EB, Chance PF (2005)

In: Nature Genetics, 37(10).

Research article (journal)

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Behr Syndrome - Complicated hereditary infantile optic atrophy Kleffner I., Meyer C., Gess B., Korsukewitz C., Allkemper T., Schirmacher A., Young P., Husstedt I. (2013) In: Klinische Neurophysiologie, 44(1). Research article (journal)
Interaction of BDNF and COMT polymorphisms on paired-associative stimulation-induced cortical plasticity. Witte AV, Kürten J, Jansen S, Schirmacher A, Brand E, Sommer J, Flöel A (2012) In: Journal of Neuroscience, 32(13). Research article (journal)
Enhanced rapid-onset cortical plasticity in CADASIL as a possible mechanism of preserved cognition. List J, Duning T, Meinzer M, Kürten J, Schirmacher A, Deppe M, Evers S, Young P, Flöel A (2011) In: Cerebral cortex, 21(12). Research article (journal)
Specific pattern of early white-matter changes in pure hereditary spastic paraplegia. Duning T, Warnecke T, Schirmacher A, Schiffbauer H, Lohmann H, Mohammadi S, Young P, Deppe M (2010) In: Movement Disorders, 25(12). Research article (journal)
A novel splice site mutation in the SPG7 gene causing widespread fiber damage in homozygous and heterozygous subjects. Warnecke T, Duning T, Schirmacher A, Mohammadi S, Schwindt W, Lohmann H, Dziewas R, Deppe M, Ringelstein EB, Young P (2010) In: Movement Disorders, 25(4). Research article (journal)
Autosomal-dominant striatal degeneration is caused by a mutation in the phosphodiesterase 8B gene. Appenzeller S, Schirmacher A, Halfter H, Bäumer S, Pendziwiat M, Timmerman V, De Jonghe P, Fekete K, Stögbauer F, Lüdemann P, Hund M, Quabius ES, Ringelstein EB, Kuhlenbäumer G (2010) In: American Journal of Human Genetics, 86(1). Research article (journal)
Four novel mutations of the myelin protein zero gene presenting as a mild and late-onset polyneuropathy. Kleffner I, Schirmacher A, Gess B, Boentert M, Young P (2010) In: Journal of Neurology, 257(11). Research article (journal)
Norepinephrine transporter (NET) promoter and 5'-UTR polymorphisms: association analysis in panic disorder. Lee YJ, Hohoff C, Domschke K, Sand P, Kuhlenbäumer G, Schirmacher A, Freitag CM, Meyer J, Stöber G, Franke P, Nöthen MM, Fritze J, Fimmers R, Garritsen HS, Stögbauer F, Deckert J (2005) In: Neuroscience Letters, 377(1). Research article (journal)
Mutations in SEPT9 cause hereditary neuralgic amyotrophy. Kuhlenbäumer G, Hannibal MC, Nelis E, Schirmacher A, Verpoorten N, Meuleman J, Watts GD, De Vriendt E, Young P, Stögbauer F, Halfter H, Irobi J, Goossens D, Del-Favero J, Betz BG, Hor H, Kurlemann G, Bird TD, Airaksinen E, Mononen T, Serradell AP, Prats JM, Van Broeckhoven C, De Jonghe P, Timmerman V, Ringelstein EB, Chance PF (2005) In: Nature Genetics, 37(10). Research article (journal)
Association of migraine with genetic variants of the NOTCH3 gene Evers S, Schwaag S, Frese A, Schirmacher A, Kuhlenbaumer G (2005) In: Cephalalgia, 25(10). Research article (journal)